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Adenomatous Polyposis Coli (APC) (Middle Region) Peptid

APC Reaktivität: Human Wirt: Synthetic BP, WB
Produktnummer ABIN5512735
  • Target Alle APC Produkte
    APC (Adenomatous Polyposis Coli (APC))
    Protein Region
    Middle Region
    Spezies
    Human
    Quelle
    • 3
    Synthetic
    Applikation
    Blocking Peptide (BP), Western Blotting (WB)
    Sequenz
    SETFDNIDNL SPKASHRSKQ RHKQSLYGDY VFDTNRHDDN RSDNFNTGNM
    Produktmerkmale
    This is a synthetic peptide designed for use in combination with anti-APC Antibody. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
  • Applikationshinweise
    Optimal working dilution should be determined by the investigator.
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Lyophilized
    Rekonstitution
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Target
    APC (Adenomatous Polyposis Coli (APC))
    Synonyme
    dp2 Peptide, dp3 Peptide, fap Peptide, fpc Peptide, xapc Peptide, dp2.5 Peptide, AI047805 Peptide, AU020952 Peptide, AW124434 Peptide, CC1 Peptide, Min Peptide, mAPC Peptide, BTPS2 Peptide, DP2 Peptide, DP2.5 Peptide, DP3 Peptide, GS Peptide, PPP1R46 Peptide, RATAPC Peptide, APC1 Peptide, APC, WNT signaling pathway regulator Peptide, adenomatous polyposis coli Peptide, adenomatous polyposis coli protein, putative Peptide, adenomatosis polyposis coli Peptide, adenomatous polyposis coli L homeolog Peptide, APC Peptide, apc Peptide, Smp_139190 Peptide, Apc Peptide, apc.L Peptide
    Hintergrund
    This gene encodes a tumor suppressor protein that acts as an antagonist of the Wnt signaling pathway. It is also involved in other processes including cell migration and adhesion, transcriptional activation, and apoptosis. Defects in this gene cause familial adenomatous polyposis (FAP), an autosomal dominant pre-malignant disease that usually progresses to malignancy. Disease-associated mutations tend to be clustered in a small region designated the mutation cluster region (MCR) and result in a truncated protein product.

    Alias Symbols: GS, DP2, DP3, BTPS2, DP2.5, PPP1R46

    Protein Size: 1304
    Gen-ID
    324
    NCBI Accession
    NM_000038, NP_000029
    UniProt
    E9PFT7
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